"IDH2-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 158664	NM_002168.4(IDH2):c.1304C>T (p.Thr435Met)	IDH2 (T383M +2 more)	Single nucleotide variant (missense variant)	D-2-hydroxyglutaric aciduria 2 +4 more	GConflicting classifications of pathogenicity
Select item 758347	NM_002168.4(IDH2):c.942T>C (p.Asp314=)	IDH2	Single nucleotide variant (synonymous variant)	IDH2-related disorder +1 more	GBenign/Likely benign
Select item 158667	NM_002168.4(IDH2):c.939A>G (p.Gly313=)	IDH2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 211177	NM_002168.4(IDH2):c.782G>A (p.Arg261His)	IDH2 (R209H +2 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 2200344	NM_002168.4(IDH2):c.519C>T (p.His173=)	IDH2	Single nucleotide variant (synonymous variant)	D-2-hydroxyglutaric aciduria 2 +1 more	GLikely benign
Select item 3034645	NM_002168.4(IDH2):c.261A>C (p.Pro87=)	IDH2	Single nucleotide variant (synonymous variant +1 more)	IDH2-related disorder	GLikely benign
Select item 559362	NM_002168.4(IDH2):c.23T>C (p.Val8Ala)	IDH2, IDH2-DT (V8A)	Single nucleotide variant (non-coding transcript variant +2 more)	D-2-hydroxyglutaric aciduria 2 +1 more	GConflicting classifications of pathogenicity

ClinVar